Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
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The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular traffickingInhibitory effects of vinpocetine on the progression of atherosclerosis are mediated by Akt/NF-κB dependent mechanisms in apoE-/- miceThe poison Dart frog's batrachotoxin modulates Nav1.8.Varicella-zoster viruses associated with post-herpetic neuralgia induce sodium current density increases in the ND7-23 Nav-1.8 neuroblastoma cell line.Physiological and genetic analysis of multiple sodium channel variants in a model of genetic absence epilepsyVinpocetine reduces carrageenan-induced inflammatory hyperalgesia in mice by inhibiting oxidative stress, cytokine production and NF-κB activation in the paw and spinal cord.Blocking Scn10a channels in heart reduces late sodium current and is antiarrhythmic.Animal toxins can alter the function of Nav1.8 and Nav1.9.Characterization of Endogenous Sodium Channels in the ND7-23 Neuroblastoma Cell Line: Implications for Use as a Heterologous Ion Channel Expression System Suitable for Automated Patch Clamp ScreeningThe sodium channel Nav1.5a is the predominant isoform expressed in adult mouse dorsal root ganglia and exhibits distinct inactivation properties from the full-length Nav1.5 channel.Isoflurane inhibits the tetrodotoxin-resistant voltage-gated sodium channel Nav1.8.Characterization of inhibitors of phosphodiesterase 1C on a human cellular system.Functional role of the C-terminus of voltage-gated sodium channel Na(v)1.8.Electrophysiological and Pharmacological Analyses of Nav1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System.Lidocaine promotes the trafficking and functional expression of Na(v)1.8 sodium channels in mammalian cells.An update on vinpocetine: New discoveries and clinical implications.Vinpocetine modulates metabolic activity and function during retinal ischemia.Effect of piracetam, vincamine, vinpocetine, and donepezil on oxidative stress and neurodegeneration induced by aluminum chloride in rats
P2860
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P2860
Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
2003年论文
@zh
2003年论文
@zh-cn
name
Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
@en
type
label
Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
@en
prefLabel
Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
@en
P2093
P356
P1476
Vinpocetine is a potent blocker of rat NaV1.8 tetrodotoxin-resistant sodium channels.
@en
P2093
James Crona
Maureen Maguire
Tony Priestley
Xiao-Wei Dong
Xiaoping Zhou
P304
P356
10.1124/JPET.103.051086
P407
P577
2003-05-01T00:00:00Z